Cargando…
Preliminary evaluation of miR-1307-3p in human serum for detection of 13 types of solid cancer using microRNA chip
Early detection and treatment are crucial for increasing the five-year survival rates of various cancers. Low-cost and convenient cancer screening tests are also critically important. Circulating microRNAs are reported as potential biomarkers for various cancers. Recently, miR-1307-3p was found to b...
Autores principales: | , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Elsevier
2021
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8441074/ https://www.ncbi.nlm.nih.gov/pubmed/34541347 http://dx.doi.org/10.1016/j.heliyon.2021.e07919 |
_version_ | 1783752802012495872 |
---|---|
author | Hashimoto, Koji Inada, Mika Yamamoto, Yusuke Ochiya, Takahiro |
author_facet | Hashimoto, Koji Inada, Mika Yamamoto, Yusuke Ochiya, Takahiro |
author_sort | Hashimoto, Koji |
collection | PubMed |
description | Early detection and treatment are crucial for increasing the five-year survival rates of various cancers. Low-cost and convenient cancer screening tests are also critically important. Circulating microRNAs are reported as potential biomarkers for various cancers. Recently, miR-1307-3p was found to be a cancer-related microRNA. We evaluated the expression levels of miR-1307-3p in sera obtained from 254 patients with thirteen types of cancer (colon cancer, lung cancer, gastric cancer, liver cancer, bladder cancer esophageal cancer, breast cancer, ovarian cancer, prostate cancer, pancreatic cancer, biliary tract cancer, brain cancer, sarcoma) and 27 non-cancer samples using isothermal amplification and microRNA chip. The expression levels of miR-1307-3p in sera obtained from cancer patients were clearly different from those obtained from non-cancer samples and differentiated the validation cohort into cancer patients and non-cancer control with high accuracy (AUC: 0.98; sensitivity: 0.98; specificity: 0.85). These results showed the potential relevance of miR-1307-3p in serum for the development of new diagnostic examination tools for cancer patients. |
format | Online Article Text |
id | pubmed-8441074 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | Elsevier |
record_format | MEDLINE/PubMed |
spelling | pubmed-84410742021-09-17 Preliminary evaluation of miR-1307-3p in human serum for detection of 13 types of solid cancer using microRNA chip Hashimoto, Koji Inada, Mika Yamamoto, Yusuke Ochiya, Takahiro Heliyon Research Article Early detection and treatment are crucial for increasing the five-year survival rates of various cancers. Low-cost and convenient cancer screening tests are also critically important. Circulating microRNAs are reported as potential biomarkers for various cancers. Recently, miR-1307-3p was found to be a cancer-related microRNA. We evaluated the expression levels of miR-1307-3p in sera obtained from 254 patients with thirteen types of cancer (colon cancer, lung cancer, gastric cancer, liver cancer, bladder cancer esophageal cancer, breast cancer, ovarian cancer, prostate cancer, pancreatic cancer, biliary tract cancer, brain cancer, sarcoma) and 27 non-cancer samples using isothermal amplification and microRNA chip. The expression levels of miR-1307-3p in sera obtained from cancer patients were clearly different from those obtained from non-cancer samples and differentiated the validation cohort into cancer patients and non-cancer control with high accuracy (AUC: 0.98; sensitivity: 0.98; specificity: 0.85). These results showed the potential relevance of miR-1307-3p in serum for the development of new diagnostic examination tools for cancer patients. Elsevier 2021-09-02 /pmc/articles/PMC8441074/ /pubmed/34541347 http://dx.doi.org/10.1016/j.heliyon.2021.e07919 Text en © 2021 The Authors https://creativecommons.org/licenses/by-nc-nd/4.0/This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/). |
spellingShingle | Research Article Hashimoto, Koji Inada, Mika Yamamoto, Yusuke Ochiya, Takahiro Preliminary evaluation of miR-1307-3p in human serum for detection of 13 types of solid cancer using microRNA chip |
title | Preliminary evaluation of miR-1307-3p in human serum for detection of 13 types of solid cancer using microRNA chip |
title_full | Preliminary evaluation of miR-1307-3p in human serum for detection of 13 types of solid cancer using microRNA chip |
title_fullStr | Preliminary evaluation of miR-1307-3p in human serum for detection of 13 types of solid cancer using microRNA chip |
title_full_unstemmed | Preliminary evaluation of miR-1307-3p in human serum for detection of 13 types of solid cancer using microRNA chip |
title_short | Preliminary evaluation of miR-1307-3p in human serum for detection of 13 types of solid cancer using microRNA chip |
title_sort | preliminary evaluation of mir-1307-3p in human serum for detection of 13 types of solid cancer using microrna chip |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8441074/ https://www.ncbi.nlm.nih.gov/pubmed/34541347 http://dx.doi.org/10.1016/j.heliyon.2021.e07919 |
work_keys_str_mv | AT hashimotokoji preliminaryevaluationofmir13073pinhumanserumfordetectionof13typesofsolidcancerusingmicrornachip AT inadamika preliminaryevaluationofmir13073pinhumanserumfordetectionof13typesofsolidcancerusingmicrornachip AT yamamotoyusuke preliminaryevaluationofmir13073pinhumanserumfordetectionof13typesofsolidcancerusingmicrornachip AT ochiyatakahiro preliminaryevaluationofmir13073pinhumanserumfordetectionof13typesofsolidcancerusingmicrornachip |